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Dopamine hydrochloride

Dopamine hydrochloride Structure
CAS No.
62-31-7
Chemical Name:
Dopamine hydrochloride
Synonyms
DOPAMINE HYDROCHLORIDE;DOPAMINE HCL;2-(3,4-DIHYDROXYPHENYL)ETHYLAMINE HYDROCHLORIDE;ASL-279;intropin;Dopamin Hcl;dopaminechloride;DOPAMINE HCL(RG);Dopamine solution;3-Hydroxytyramine, HCl
CBNumber:
CB9243534
Molecular Formula:
C8H12ClNO2
Molecular Weight:
189.64
MOL File:
62-31-7.mol
Modify Date:
2024/8/8 13:40:43

Dopamine hydrochloride Properties

Melting point 248-250 °C(lit.)
Density 1.4 g/cm3
Flash point 11℃
storage temp. Store below +30°C.
solubility alcohol: 20 mg/mL
form Crystalline Powder
color light tan
Water Solubility soluble
Sensitive Air & Light Sensitive
Merck 14,8462
BRN 3656720
Stability Stable. Incompatible with strong oxidizing agents. Combustible.
InChIKey CTENFNNZBMHDDG-UHFFFAOYSA-N
CAS DataBase Reference 62-31-7(CAS DataBase Reference)
EPA Substance Registry System 1,2-Benzenediol, 4-(2-aminoethyl)-, hydrochloride (62-31-7)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P301+P312+P330
Hazard Codes  Xi,N,Xn,T,F
Risk Statements  36/37/38-50/53-22-39/23/24/25-23/24/25-11
Safety Statements  26-36-61-45-36/37-16
RIDADR  UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany  2
RTECS  UX1092000
8-10-23
Hazard Note  Irritant
TSCA  Yes
HS Code  29222900
Toxicity LD50 orally in Rabbit: 2859 mg/kg
NFPA 704
1
0 0

Dopamine hydrochloride price More Price(13)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) H8502 Dopamine hydrochloride 62-31-7 5G ₹2392.33 2022-06-14 Buy
Sigma-Aldrich(India) H8502 Dopamine hydrochloride 62-31-7 10G ₹4394.95 2022-06-14 Buy
Sigma-Aldrich(India) H8502 Dopamine hydrochloride 62-31-7 25G ₹8064.63 2022-06-14 Buy
Sigma-Aldrich(India) PHR1090 Dopamine hydrochloride Pharmaceutical Secondary Standard; Certified Reference Material 62-31-7 1G ₹8465.15 2022-06-14 Buy
Sigma-Aldrich(India) H8502 Dopamine hydrochloride 62-31-7 100G ₹47132.05 2022-06-14 Buy
Product number Packaging Price Buy
H8502 5G ₹2392.33 Buy
H8502 10G ₹4394.95 Buy
H8502 25G ₹8064.63 Buy
PHR1090 1G ₹8465.15 Buy
H8502 100G ₹47132.05 Buy

Dopamine hydrochloride Chemical Properties,Uses,Production

Description

Dopamine (hydrochloride) is an endogenous catecholamine neurotransmitter synthesized from the amino acid L-tyrosine that acts as an agonist at dopamine receptors (D1-5). Dopamine is mainly synthesized in the substantia nigra and ventral tegmental area, and is a precursor in norepinephrine and epinephrine biosynthesis. Dopamine-containing neurons in the brain are involved in reward-motivated behavior, motor control, and hormone release. Dopamine is also synthesized in the adrenal glands where it exerts peripheral paracrine functions including control of vasodilation, sodium excretion, insulin production, gastrointestinal motility, and the activity of lymphocytes. Loss or damage of dopaminergic neurons in the substantia nigra is associated with Parkinson’s disease.

Chemical Properties

Dopamine hydrochloride is designated chemically as 3,4-dihydroxyphenethylamine hydrochloride, a white crystalline powder freely soluble in water. It can also be dissolved in hot 95% ethanol, methanol, and sodium hydroxide solution. However, it is insoluble in chloroform, ether, and benzene. It has no odor and a slightly bitter taste. Dopamine (also referred to as 3-hydroxytyramine) is a naturally occurring biochemical catecholamine precursor of norepinephrine.

Uses

Endogenous catecholamine with α and β-adrenergic activity. Cardiotonic; antihypotensive.

Indications

Dopamine HCl is indicated for the correction of hemodynamic imbalances present in the shock syndrome due to myocardial infarction, trauma, endotoxic septicemia, open-heart surgery, renal failure, and chronic cardiac decompensation as in congestive failure.

Application

Dopamine hydrochloride has been used to study dopamine-mediated transient modulation of the physiological responses in whiteleg shrimp, Litopenaeus vannamei.
It has been used to study dopamine-mediated changes in immunity susceptibility to Lactococcus garvieae in the freshwater giant prawn, Macrobrachium rosenbergii.
It has been used to study the molecular link between dopamine-induced oxidative stress and mHtt (mutant Huntingtin) toxicity in relation to the activation of the autophagy pathway in an 'in vitro' model of parkinsonian Huntington's Disease.

Preparation

Dopamine hydrochloride is produced through the ring-opening reaction of piperonyl ethylamine. Piperethylamine and phenol are added to a reaction vessel and cooled down. Hydrochloric acid is slowly added while heating up the mixture to 110°C, and refluxed for 12-44 hours until the reaction reaches completion. The solution is then slightly cooled and water is added, and the mixture is stirred well and allowed to separate into layers. The upper phenolic layer is then removed, and the aqueous layer is extracted with isopropyl acetate. The extracted aqueous layer is then evaporated under reduced pressure (8.0kPa) until dry. Half the amount of ethanol and hydrochloric acid are added to the dry residue and heated to dissolve. The solution is then cooled, crystallized, and filtered. The filter cake is washed with ethanol and dried to obtain the final product, with a yield of 74%.

General Description

Dopamine Hydrochloride is the hydrochloride salt form of dopamine, a monoamine compound with positive inotropic activity. Dopamine is a neurotransmitter which is a naturally occurring catecholamine. Dopamine hydrochloride salt is indicated as a medicine for the treatment of acute congestive and renal failures.

Biological Activity

Endogenous neurotransmitter that acts as an agonist at dopamine D 1-5 receptors. Synthesized in the substantia nigra and ventral tegmental area, and is a precursor in noradrenalin and adrenalin biosynthesis.

Pharmacokinetics

Dopamine hydrochloride(62-31-7) is a precursor for the synthesis of epinephrine in the body. It has β (mainly β1 receptor) receptor agonism and α receptor agonism, and can also promote the release of norepinephrine. It can enhance myocardial contractility, increase cardiac output, and accelerate the heart rate to a lesser extent (not as obvious as isoproterenol); stimulate the α-receptors of blood vessels in tissues such as skin and muscles, so that blood vessels constrict and blood supply is reduced; it stimulates visceral blood vessels ( The dopamine receptors in the kidney, mesentery, and heart) dilate and increase blood flow. The change of total peripheral resistance is not obvious, but it is beneficial to improve the blood supply of vital organs during shock.

Dopamine hydrochloride Preparation Products And Raw materials

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